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Journal Abstract Search

249 related items for PubMed ID: 5008795

  • 1. Screening tests and chromatography for the detection of inborn errors of metabolism.
    Stuber A.
    Clin Chim Acta; 1972 Feb; 36(2):309-13. PubMed ID: 5008795
    [No Abstract] [Full Text] [Related]

  • 2. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.
    Yahya NA, Ismail Z, Embong KH, Mohamad SA.
    Southeast Asian J Trop Med Public Health; 1995 Feb; 26 Suppl 1():130-3. PubMed ID: 8629091
    [Abstract] [Full Text] [Related]

  • 3. A guide to screening newborn infants for inborn errors of metabolism.
    Buist NR, Jhaveri BM.
    J Pediatr; 1973 Mar; 82(3):511-22. PubMed ID: 4266933
    [No Abstract] [Full Text] [Related]

  • 4. Urinary screening tests in the infant and young child.
    Bradley GM.
    Hum Pathol; 1971 Jun; 2(2):309-20. PubMed ID: 4256386
    [No Abstract] [Full Text] [Related]

  • 5. Screening for metabolic disorders associated with mental retardation.
    Hill A, Zaleski WA.
    Clin Biochem; 1972 Mar; 5(1):33-45. PubMed ID: 5022447
    [No Abstract] [Full Text] [Related]

  • 6. [Early detection of congenital metabolic anomalies].
    Thalhammer O.
    Klin Padiatr; 1973 Mar; 185(2):81-90. PubMed ID: 4576950
    [No Abstract] [Full Text] [Related]

  • 7. [Aminoaciduria screening in newborn infants using, comparatively, chromatographic and colorimetric methods].
    Pedrazzi AH, Rossi AR.
    Rev Farm Bioquim Univ Sao Paulo; 1976 Mar; 14(2):241-54. PubMed ID: 1030516
    [Abstract] [Full Text] [Related]

  • 8. [Methods of thin-layer chromatography for the identification of aminoaciduria, aminoacidemia and galactosemia].
    Bremer HJ, Nützenadel W, Bickel H.
    Monatsschr Kinderheilkd (1902); 1969 Jan; 117(1):32-7. PubMed ID: 5408275
    [No Abstract] [Full Text] [Related]

  • 9. Set of simple side-room urine tests for detection of inborn errors of metabolism.
    Buist NR.
    Br Med J; 1968 Jun 22; 2(5607):745-9. PubMed ID: 4231911
    [No Abstract] [Full Text] [Related]

  • 10. Screening for disorders of amino acid metabolism by thin-layer high voltage electrophoresis.
    Farrelly RO, Watkins WB.
    Clin Chim Acta; 1968 May 22; 20(2):291-4. PubMed ID: 4297715
    [No Abstract] [Full Text] [Related]

  • 11. Screening for organic acidurias and amino acidopathies in newborns and children.
    Chalmers RA, Purkiss P, Watts RW, Lawson AM.
    J Inherit Metab Dis; 1980 May 22; 3(2):27-43. PubMed ID: 6777599
    [No Abstract] [Full Text] [Related]

  • 12. A simple screening method for detecting isovalerylglycine in urine patients with isovaleric acidemia.
    Ando T, Nyhan WL.
    Clin Chem; 1970 May 22; 16(5):420-2. PubMed ID: 5443766
    [No Abstract] [Full Text] [Related]

  • 13. [Chromatography of amino acids on a thin layer of cellulose in urine exminations in inborn errors of metabolism].
    Hyánek J.
    Cas Lek Cesk; 1969 Nov 22; 108(49):1479-81. PubMed ID: 5357423
    [No Abstract] [Full Text] [Related]

  • 14. [Detection of metabolic diseases].
    Adriaenssens K, Van Sande M.
    Acta Neurol Psychiatr Belg; 1968 Oct 22; 68(10):719-28. PubMed ID: 4976725
    [No Abstract] [Full Text] [Related]

  • 15. [Screening for congenital metabolic disorders].
    Knapp A, Machill G.
    Kinderarztl Prax; 1974 Jun 22; 42(6):270-7. PubMed ID: 4610264
    [No Abstract] [Full Text] [Related]

  • 16. Detection of metabolic disorders. Chromatographic procedures and interpretation of results.
    Berry HK, Leonard C, Peters H, Granger M, Chunekamrai N.
    Clin Chem; 1968 Nov 22; 14(11):1033-65. PubMed ID: 4972564
    [No Abstract] [Full Text] [Related]

  • 17. SOME AIDS IN THE DIAGNOSIS OF GENETIC DISORDERS.
    CHUTE AL.
    Can Med Assoc J; 1965 Aug 07; 93(6):260-5. PubMed ID: 14328042
    [Abstract] [Full Text] [Related]

  • 18. Application of a thin-layer chromatography microtechnique for the screening of aminoacidurias in 3,165 Chinese newborns.
    Wang TR.
    Taiwan Yi Xue Hui Za Zhi; 1984 Sep 07; 83(9):869-78. PubMed ID: 6596395
    [No Abstract] [Full Text] [Related]

  • 19. Problems in screening infants for defects of amino acid metabolism.
    Jackson SH.
    Clin Biochem; 1973 Mar 07; 6(1):15-21. PubMed ID: 4121648
    [No Abstract] [Full Text] [Related]

  • 20. High-voltage electrophoresis in urinary amino acid screening.
    Holmgren G, Jeppson JO, Samuelson G.
    Scand J Clin Lab Invest; 1970 Dec 07; 26(4):313-8. PubMed ID: 5486398
    [No Abstract] [Full Text] [Related]

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